tert-Butyl 4-(3-nitropyridin-2-yl)piperazine-1-carboxylate
95%
- Product Code: 46236
Alias:
1-Boc-4-(3-nitropyridin-2-yl)piperazine
CAS:
153473-24-6
| Molecular Weight: | 308.33 g./mol | Molecular Formula: | C₁₄H₂₀N₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09028514 | |
| Melting Point: | Boiling Point: | 447.8°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperazine ring and a nitropyridine moiety, makes it valuable for constructing compounds with potential therapeutic applications, particularly in the fields of central nervous system (CNS) disorders and oncology. Researchers often employ it to create derivatives that can interact with specific receptors or enzymes, aiding in the discovery of new drugs. Additionally, its tert-butyl group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,798.00 |
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| 1.000 | 10-20 days | ฿9,198.00 |
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tert-Butyl 4-(3-nitropyridin-2-yl)piperazine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperazine ring and a nitropyridine moiety, makes it valuable for constructing compounds with potential therapeutic applications, particularly in the fields of central nervous system (CNS) disorders and oncology. Researchers often employ it to create derivatives that can interact with specific receptors or enzymes, aiding in the discovery of new drugs. Additionally, its tert-butyl group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry.
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